| Primary Device ID | 08132500167418 |
| NIH Device Record Key | 7049ad76-9065-4e1a-b6c8-1dc6df103377 |
| Commercial Distribution Discontinuation | 2020-08-13 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | cannulaSideKick |
| Version Model Number | RFK-C101020S-ZK |
| Company DUNS | 184200736 |
| Company Name | COSMAN MEDICAL, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |